29 Oct
Lifelancer
Junagadh
About the JobSkills We Are Hiring Regulatory Affairs For Pharmaceutical company Location: Bodakdev Ahmedabad. Qualification: B.Pharm M.Pharm DPharm Experience:2 to 3 Years In Regulatory Documentation Salary:20k to 25k CTC Job Responsibility: Preparation Review of Dossiers in ACTD CTD or Country specific format for ROW market. Preparation and submission of Site GMP Application Product Registration Applications with respective Regulatory Authorities. Liasoning with Local FDA for Product Permission FSC COPP etc. CDSCO for inclusion of COPP. Coordination with QA/QC departments for technical/legal documents.
Artwork designing for registration sample preparation and submission Preparation and/or review of technical documents such as BMR PVP/PVR Specification MOA COA of raw material finished product and packing materials and all other documents for compilation of dossiers. Documents preparation for bidding in National International Tenders MOH query response and resolution within stipulated timeline Lifelancer ( ) is a talenthiring platform in Life Sciences Pharma and IT. The platform connects talent with opportunities in pharma biotech health sciences healthtech data science and IT domains. Please use the below Lifelancer link for job application and quicker response. /jobs/view/cc524b97bd6bdfd81636f Remote Work : No
▶️ Regulatory Affairs
🖊️ Lifelancer
📍 Junagadh